A contrast of Pb(II), Cd(II), and Cu(II) toxicities to Aspergillus niger through biochemical, morphological, and genetic investigations

Lin Zhang, Xin Yang, Sensen Li, Lingyi Tang, Tianyi Chen, Tingting Gu, Genqiang Chen, Geoffrey Michael Gadd (Lead / Corresponding author), Zhen Li (Lead / Corresponding author)

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    11 Citations (Scopus)
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    Abstract

    The toxicity of metals to microorganisms is highly correlated with the type of metal used. However, the differences in the resistance mechanisms of filamentous fungi to multiple metals remain unclear. In this study, we investigated the responses of Aspergillus niger to three toxic metals, i.e., Pb 2+, Cd 2+, and Cu 2+. Fungal growth and metabolism indices showed that A. niger had a higher tolerance to Pb 2+ (>1000 mg L −1) than to Cu 2+ (300 mg L −1) and Cd 2+ (50 mg L −1). An appropriate Pb 2+ concentration (<500 mg L −1) stimulated fungal growth and metabolic activity, whereas Cd 2+ and Cu 2+ stress showed continuously negative influences on fungal physiological parameters, such as biomass and secretion of oxalic acid. A. niger responded to Pb stress by constructing a new border layer around its cell wall. This pathway was also confirmed using RNA-seq analysis, i.e., the gene encoding cell wall α-1,3-glucan synthase was upregulated. This upregulation subsequently promoted the production of polysaccharides, which are the main components that support fungal cell walls. In contrast, the expression of genes encoding both AAA family ATPase and efflux pump antibiotic resistance proteins for Cd 2+ and Cu 2+ was significantly downregulated. Therefore, these findings elucidated the relatively complete fungal responses to different metal stresses.

    Original languageEnglish
    Article number130691
    Number of pages9
    JournalJournal of Hazardous Materials
    Volume446
    Early online date28 Dec 2022
    DOIs
    Publication statusPublished - 15 Mar 2023

    Keywords

    • A. niger
    • Metal toxicity
    • Physiological response
    • Cell morphology change
    • RNA-seq analysis

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